Canonical Allele Identifier: CA1590664604

Gene: PPARGC1B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149814922C= , CM000667.2:g.149814922C=	GRCh38
NC_000005.9:g.149194485C= , CM000667.1:g.149194485C=	GRCh37
NC_000005.8:g.149174678C=	NCBI36
NG_016747.1:g.89671C=

Transcript Alleles

HGVS	Amino-acid Change
NM_133263.4:c.79-5511C= MANE Select	NP_573570.3:n.79-5511C=
ENST00000309241.10:c.79-5511C= MANE Select	ENSP00000312649.5:n.79-5511C=
NM_001172698.1:c.79-5511C=	NP_001166169.1:n.79-5511C=
NM_001172698.2:c.79-5511C=	NP_001166169.1:n.79-5511C=
NM_001172699.1:c.4-5511C=	NP_001166170.1:n.4-5511C=
NM_001172699.2:c.4-5511C=	NP_001166170.1:n.4-5511C=
NM_133263.3:c.79-5511C=	NP_573570.3:n.79-5511C=
ENST00000309241.9:c.79-5511C=	ENSP00000312649.5:n.79-5511C=
ENST00000360453.8:c.79-5511C=	ENSP00000353638.4:n.79-5511C=
ENST00000394320.7:c.79-5511C=	ENSP00000377855.3:n.79-5511C=
ENST00000403750.5:c.4-5511C=	ENSP00000384403.1:n.4-5511C=
ENST00000461780.1:n.433-2691C=
XM_011537553.1:c.79-5511C=	XP_011535855.1:n.79-5511C=
XM_011537553.2:c.79-5511C=	XP_011535855.1:n.79-5511C=
XM_011537555.1:c.79-5511C=	XP_011535857.1:n.79-5511C=
XM_011537555.2:c.79-5511C=	XP_011535857.1:n.79-5511C=
XM_011537557.1:c.79-5511C=	XP_011535859.1:n.79-5511C=